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Description
Mitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N-terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO), Alpers-Huttenlocher syndrome (AHS), and mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq
Specifications
Specifications
| Antigen | POLG |
| Applications | Flow Cytometry, Immunofluorescence, Immunohistochemistry, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | polymerase (DNA directed), gamma |
| Formulation | In PBS (0.09% sodium azide) |
| Gene | POLG |
| Gene Alias | FLJ27114, MDP1, PEO, POLG1, POLGA, SANDO, SCAE |
| Gene Symbols | POLG |
| Host Species | Rabbit |
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